FDA-Drug2014-12-03Class II
5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7941-09.
Hospira Inc.
Hazard
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
Sold states
Nationwide, Puerto Rico, and U.S. Virgin Islands.
Affected count
340,272 bags
Manufactured in
275 N Field Dr, N/A, Lake Forest, IL, United States
Products
5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7941-09.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0282-2015Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief